Structure–activity relationships of dimeric PPAR agonists von Sauerberg, Per, Mogensen, John P., Jeppesen, Lone, Svensson, L. Anders, Fleckner, Jan, Nehlin, Jan, Wulff, Erik M., Pettersson, Ingrid

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Novel Tricyclic-α-alkyloxyphenylpropionic Acids:  Dual PPARα/γ Agonists with Hypolipidemic and Antidiabetic Activity von Sauerberg, Per, Pettersson, Ingrid, Jeppesen, Lone, Bury, Paul S, Mogensen, John P, Wassermann, Karsten, Brand, Christian L, Sturis, Jeppe, Wöldike, Helle F, Fleckner, Jan, Andersen, Anne-Sofie T, Mortensen, Steen B, Svensson, L. Anders, Rasmussen, Hanne B, Lehmann, Søren V, Polivka, Zdenek, Sindelar, Karel, Panajotova, Vladimira, Ynddal, Lars, Wulff, Erik M

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Identification and Synthesis of a Novel Selective Partial PPARδ Agonist with Full Efficacy on Lipid Metabolism In Vitro and In Vivo von Sauerberg, Per, Olsen, Grith S, Jeppesen, Lone, Mogensen, John P, Pettersson, Ingrid, Jeppesen, Claus B, Daugaard, Jens R, Galsgaard, Elisabeth D, Ynddal, Lars, Fleckner, Jan, Panajotova, Vladimira, Polivka, Zdenek, Pihera, Pavel, Havranek, Miroslav, Wulff, Erik M

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Selective PPAR Agonists for the Treatment of Type 2 Diabetes von NEHLIN, JAN O., MOGENSEN, JOHN P., PETTERSON, INGRID, JEPPESEN, LONE, FLECKNER, JAN, WULFF, ERIK M., SAUERBERG, PER

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Novel selective PPARδ agonists: Optimization of activity by modification of alkynylallylic moiety von Havranek, Miroslav, Sauerberg, Per, Mogensen, John P., Kratina, Pavel, Jeppesen, Claus B., Pettersson, Ingrid, Pihera, Pavel

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Design of a partial PPARδ agonist von Pettersson, Ingrid, Ebdrup, Søren, Havranek, Miroslav, Pihera, Pavel, Kořínek, Marek, Mogensen, John P., Jeppesen, Claus B., Johansson, Eva, Sauerberg, Per

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6-Chloro-3-alkylamino-4H-thieno[3,2-e]-1,2,4-thiadiazine 1,1-Dioxide Derivatives Potently and Selectively Activate ATP Sensitive Potassium Channels of Pancreatic β-Cells von Nielsen, Flemming E, Bodvarsdottir, Thora B, Worsaae, Anne, MacKay, Peter, Stidsen, Carsten E, Boonen, Harrie C. M, Pridal, Lone, Arkhammar, Per O. G, Wahl, Philip, Ynddal, Lars, Junager, Finn, Dragsted, Nils, Tagmose, Tina M, Mogensen, John P, Koch, Anette, Treppendahl, Svend P, Hansen, J. Bondo

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Design of potent PPARα agonists von Sauerberg, Per, Mogensen, John P., Jeppesen, Lone, Bury, Paul S., Fleckner, Jan, Olsen, Grith S., Jeppesen, Claus B., Wulff, Erik M., Pihera, Pavel, Havranek, Miroslav, Polivka, Zdenek, Pettersson, Ingrid

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Large Dimeric Ligands with Favorable Pharmacokinetic Properties and Peroxisome Proliferator-Activated Receptor Agonist Activity in Vitro and in Vivo von Sauerberg, Per, Bury, Paul S, Mogensen, John P, Deussen, Heinz-Josef, Pettersson, Ingrid, Fleckner, Jan, Nehlin, Jan, Frederiksen, Klaus S, Albrektsen, Tatjana, Din, Nanni, Svensson, L. Anders, Ynddal, Lars, Wulff, Erik M, Jeppesen, Lone

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Design and synthesis of novel PPARα/γ/δ triple activators using a known PPARα/γ dual activator as structural template von Mogensen, John P, Jeppesen, Lone, Bury, Paul S, Pettersson, Ingrid, Fleckner, Jan, Nehlin, Jan, Frederiksen, Klaus S, Albrektsen, Tatjana, Din, Nanni, Mortensen, Steen B, Svensson, L.Anders, Wassermann, Karsten, Wulff, Erik M, Ynddal, Lars, Sauerberg, Per

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Arylcyanoguanidines as Activators of Kir6.2/SUR1KATP Channels and Inhibitors of Insulin Release von Tagmose, Tina M, Schou, Søren C, Mogensen, John P, Nielsen, Flemming E, Arkhammar, Per O. G, Wahl, Philip, Hansen, Birgit S, Worsaae, Anne, Boonen, Harrie C. M, Antoine, Marie-Hélène, Lebrun, Philippe, Hansen, John Bondo

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Synthesis and biological activity of 3,3-Diamino-sulfonylacrylonitriles as novel inhibitors of glucose induced insulin secretion from beta cells von Tagmose, Tina M, Zaragoza, Florencio, Boonen, Harrie C.M, Worsaae, Anne, Mogensen, John P, Nielsen, Flemming E, Jensen, Anette Frost, Hansen, John Bondo

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Phenylcyanoguanidines as inhibitors of glucose-induced insulin secretion from beta cells von Tagmose, Tina M, Mogensen, John P, Agerholm, Pia C, Arkhammar, Per O.G, Wahl, Philip, Worsaae, Anne, Hansen, J.Bondo

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Arylcyanoguanidines as activators of Kir6.2/SUR1K ATP channels and inhibitors of insulin release von Tagmose, Tina M, Schou, Søren C, Mogensen, John P, Nielsen, Flemming E, Arkhammar, Per O G, Wahl, Philip, Hansen, Birgit S, Worsaae, Anne, Boonen, Harrie C M, Antoine, Marie-Hélène, Lebrun, Philippe, Hansen, John Bondo

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Novel selective PPARdelta agonists: optimization of activity by modification of alkynylallylic moiety von Havranek, Miroslav, Sauerberg, Per, Mogensen, John P, Kratina, Pavel, Jeppesen, Claus B, Pettersson, Ingrid, Pihera, Pavel

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Design of a partial PPARdelta agonist von Pettersson, Ingrid, Ebdrup, Søren, Havranek, Miroslav, Pihera, Pavel, Korínek, Marek, Mogensen, John P, Jeppesen, Claus B, Johansson, Eva, Sauerberg, Per

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Identification and synthesis of a novel selective partial PPARdelta agonist with full efficacy on lipid metabolism in vitro and in vivo von Sauerberg, Per, Olsen, Grith S, Jeppesen, Lone, Mogensen, John P, Pettersson, Ingrid, Jeppesen, Claus B, Daugaard, Jens R, Galsgaard, Elisabeth D, Ynddal, Lars, Fleckner, Jan, Panajotova, Vladimira, Polivka, Zdenek, Pihera, Pavel, Havranek, Miroslav, Wulff, Erik M

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Design of potent PPARalpha agonists von Sauerberg, Per, Mogensen, John P, Jeppesen, Lone, Bury, Paul S, Fleckner, Jan, Olsen, Grith S, Jeppesen, Claus B, Wulff, Erik M, Pihera, Pavel, Havranek, Miroslav, Polivka, Zdenek, Pettersson, Ingrid

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The synthesis of new adenosine A3 selective ligands containing bioisosteric isoxazoles von MOGENSEN, J. P, ROBERTS, S. M, BOWLER, A. N, THOMSEN, C, KNUTSEN, L. J. S

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Design and synthesis of novel PPARalpha/gamma/delta triple activators using a known PPARalpha/gamma dual activator as structural template von Mogensen, John P, Jeppesen, Lone, Bury, Paul S, Pettersson, Ingrid, Fleckner, Jan, Nehlin, Jan, Frederiksen, Klaus S, Albrektsen, Tatjana, Din, Nanni, Mortensen, Steen B, Svensson, L Anders, Wassermann, Karsten, Wulff, Erik M, Ynddal, Lars, Sauerberg, Per

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